Nitrate removal, communities of denitrifiers and adverse effects in different carbon substrates for use in denitrification beds

WATER RESEARCH

卷:45

Article

Warneke, Soeren¹  Schipper, Louis A.¹  Matiasek, Michael G.²  Scow, Kate M.²  Cameron, Stewart³  Bruesewitz, Denise A.⁴  McDonald, Ian R.⁴ 

[1] Univ Waikato, Dept Earth & Ocean Sci, Hamilton, New Zealand

[2] Univ Calif Davis, Dept Land Air & Water Resources, Davis, CA 95616 USA

[3] GNS Sci, Wairakei Res Ctr, Taupo, New Zealand

[4] Univ Waikato, Dept Biol Sci, Hamilton, New Zealand

关键词: Denitrification;    Controlling factors;    Bioreactor;    Denitrification genes;    nir;   

DOI  :  10.1016/j.watres.2011.08.007

来源: Elsevier

【 摘 要 】

Denitrification beds are containers filled with wood by-products that serve as a carbon and energy source to denitrifiers, which reduce nitrate (NO3-) from point source discharges into non-reactive dinitrogen (N-2) gas. This study investigates a range of alternative carbon sources and determines rates, mechanisms and factors controlling NO3- removal, denitrifying bacterial community, and the adverse effects of these substrates. Experimental barrels (0.2 m(3)) filled with either maize cobs, wheat straw, green waste, sawdust, pine woodchips or eucalyptus woodchips were incubated at 16.8 degrees C or 27.1 degrees C (outlet temperature), and received NO3- enriched water (14.38 mg N L-1 and 17.15 mg N L-1). After 2.5 years of incubation measurements were made of NO3--N removal rates, in vitro denitrification rates (DR), factors limiting denitrification (carbon and nitrate availability, dissolved oxygen, temperature, pH, and concentrations of NO3-, nitrite and ammonia), copy number of nitrite reductase (nirS and nirK) and nitrous oxide reductase (nosZ) genes, and greenhouse gas production (dissolved nitrous oxide (N2O) and methane), and carbon (TOC) loss. Microbial denitrification was the main mechanism for NO3--N removal. Nitrate-N removal rates ranged from 1.3 (pine woodchips) to 6.2 g N m(-3) d(-1) (maize cobs), and were predominantly limited by C availability and temperature (Q(10) = 1.2) when NO3--N outlet concentrations remained above 1 mg L-1. The NO3--N removal rate did not depend directly on substrate type, but on the quantity of microbially available carbon, which differed between carbon sources. The abundance of denitrifying genes (nirS, nirK and nosZ) was similar in replicate barrels under cold incubation, but varied substantially under warm incubation, and between substrates. Warm incubation enhanced growth of nirS containing bacteria and bacteria that lacked the nosZ gene, potentially explaining the greater N2O emission in warmer environments. Maize cob substrate had the highest NO3--N removal rate, but adverse effects include TOC release, dissolved N2O release and substantial carbon consumption by non-denitrifiers. Woodchips removed less than half of NO3- removed by maize cobs, but provided ideal conditions for denitrifying bacteria, and adverse effects were not observed. Therefore we recommend the combination of maize cobs and woodchips to enhance NO3- removal while minimizing adverse effects in denitrification beds. (C) 2011 Elsevier Ltd. All rights reserved.

【 授权许可】

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